Xanthinuria
Symptom Information:
Symptom ID: | HPO:0010934 | |||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of nucleobase metabolism(HPO:0010932) Abnormality of purine metabolism(HPO:0004352) Abnormality of xanthine metabolism(HPO:0010933) Xanthinuria(HPO:0010934) MedDRA: |
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Database Frequency: | 4 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Hereditary xanthinuria | (Orphanet:3467) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
Xanthinuria type I | (Orphanet:93601) |